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Q24672101-C5CFD9BE-CC23-4070-B06E-E8FA002C08C4
Q24672101-C5CFD9BE-CC23-4070-B06E-E8FA002C08C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24672101-C5CFD9BE-CC23-4070-B06E-E8FA002C08C4
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome
P2860
Q24672101-C5CFD9BE-CC23-4070-B06E-E8FA002C08C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24672101-C5CFD9BE-CC23-4070-B06E-E8FA002C08C4
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wasDerivedFrom
90b3010e77399c63abbf2e14e7ff96cb895d21d3
P2860
Structure of the FGF receptor tyrosine kinase domain reveals a novel autoinhibitory mechanism